Status:
COMPLETED
Antagonistic Interaction CB1-paracetamol
Lead Sponsor:
University Hospital, Clermont-Ferrand
Conditions:
Pain
Eligibility:
All Genders
18-40 years
Phase:
PHASE1
Brief Summary
Evaluation of an possible inhibiting effect of Rimonabant on the analgesic effect of Paracetamol in healthy volunteers
Detailed Description
Double Blind, cross-over, randomized and controlled versus placebo, study in healthy volunteers.
Eligibility Criteria
Inclusion
- Healthy volunteers
- between 18 and 40 years old
- written consent given
Exclusion
- Rimonabant or paracetamol hypersensibility
- Excessive consumption of alcohol, tobacco, coffee, tea or toxicomania
- Concomitant medication
- Chronical diseases
Key Trial Info
Start Date :
September 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 1 2008
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT00750347
Start Date
September 1 2008
End Date
October 1 2008
Last Update
January 19 2011
Active Locations (2)
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1
CIC-CPC
Clermont-Ferrand, France, 63000
2
CHU Clermont-Ferrand
Clermont-Ferrand, France, 63003